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Dendritic cells (DCs) are Immune Cell s and form part of the Mammal ian Immune System . Their main function is to process antigen material and present it on the surface to other cells of the immune system, thus functioning as Antigen-presenting Cell s. Dendritic cells are present in small quantities in tissues that are in contact with the external environment, mainly the Skin (where they are often called Langerhans Cell s) and the inner lining of the Nose , Lung s, Stomach and Intestine s. They can also be found in an immature state in the Blood . Once activated, they migrate to the lymphoid tissues where they interact with T cells and B cells to initiate and shape the adaptive immune response. At certain development stages they grow branched projections, the '' Dendrite s'', that give the cell its name. However, these do not have any special relation with Neuron s, which also possess similar appendages. Immature dendritic cells are also called veiled cells, in which case they possess large cytoplasmic 'veils' rather than dendrites. HISTORY Dendritic cells were first described by Paul Langerhans (Langerhans cells) in the late nineteenth century. It wasn't until 1973, however, that the term "dendritic cells" was coined by Ralph M. Steinman and Zanvil A. Cohn .1 TYPES OF DENDRITIC CELLS In all dendritic cells, the similar morphology results in a very large contact surface to their surroundings compared to overall cell volume. ''In vivo'' - primate The most common division of dendritic cells is " Myeloid " vs. " Plasmacytoid " (or " Lymphoid "): The markers BDCA-2 , BDCA-3 , and BDCA-4 can be used to discriminate among the types.5 Lymphoid and myleoid DCs evolve from lymphoid or myeloid precursors respectively and thus are of Haematopoietic origin. By contrast, Follicular Dendritic Cells (FDC) are probably not of Hematopoietic origin, but simply look similar to true dendritic cells. ''In vitro'' In some respects, dendritic cells cultured In Vitro do not show the same behavior or capability as dendritic cells isolated ''ex vivo''. Nonetheless, they are often used for research as they are still much more readily available than genuine DCs.
Nonprimate While humans and non-human primates such as Rhesus Macaque s appear to have DCs divided into these groups, other species (such as the Mouse ) have different subdivisions of DCs. LIFE CYCLE Formation of immature cells Dendritic cells are derived from hemopoietic bone marrow progenitor cells. These progenitor cells initially transform into immature dendritic cells. These cells are characterized by high endocytic activity and low T-cell activation potential. Immature dendritic cells constantly sample the surrounding environment for pathogens such as s and Killer T-cell s as well as B-cell s by presenting them with antigens derived from the pathogen, alongside non-antigen specific costimulatory signals. Every helper T-cell is specific to one particular antigen. Only professional Antigen-presenting Cells (macrophages, B lymphocytes, and dendritic cells) are able to activate a helper T-cell which has never encountered its antigen before. Dendritic cells are the most potent of all the antigen-presenting cells. As mentioned above, mDC probably from Monocyte s, white blood cells which circulate in the body and, depending on the right signal, can turn into either dendritic cells or Macrophage s. Monocyte-derived dendritic cells can be generated in vitro from peripheral blood mononuclear cells (PBMCs). Plating of PBMCs in a tissue culture flask permits adherence of monocytes. Treatment of these monocytes with interleukin 4 (IL-4) and granulocyte-macrophage colony stimulating factor (GM-CSF) leads to differentiation to immature dendritic cells (iDCs) in about a week. Subsequent treatment with tumor necrosis factor alpha (TNFa) further differentiates the iDCs into mature dendritic cells. Activated dendritic cells Activated macrophages have a lifespan of only a few days. The lifespan of activated dendritic cells, while somewhat varying according to type and origin, is of a similar order of magnitude, but immature dendritic cells seem to be able to exist in an unactivated state for much longer. The monocytes in turn are formed from stem cells in the Bone Marrow . Research challenges The exact genesis and development of the different types and subsets of dendritic cells and their interrelationship is only marginally understood at the moment, as dendritic cells are so rare and difficult to isolate that only in recent years they have become subject of focused research. Distinct surface antigens that characterize dendritic cells have only become known from 2000 on; before that, researchers had to work with a 'cocktail' of several antigens which, used in combination, result in isolation of cells with characteristics unique to DCs. DENDRITIC CELLS AND CYTOKINES The dendritic cells are constantly in communication with other cells in the body. This communication can take the form of direct cell-to-cell contact based on the interaction of cell-surface proteins. An example of this includes the interaction of the receptor CD40 of the dendritic cell with CD40L present on the Lymphocyte . However, the cell-cell interaction can also take place at a distance via Cytokine s. For example, stimulating dendritic cells ''in vivo'' with microbial extracts causes the dendritic cells to rapidly begin producing IL-12 .7 IL-12 is a signal that helps send naive CD4 T cells towards a Th1 phenotype. The ultimate consequence is priming and activation of the immune system for attack against the antigens which the dendritic cell presents on its surface. However, there are differences in the cytokines produced depending on the type of dendritic cell. The plasmacytoid DC has the ability to produce huge amounts of IFN-a , more than any other blood cell.8 RELATIONSHIP TO HIV, ALLERGY, AND AUTOIMMUNE DISEASES HIV , which causes AIDS , can bind to dendritic cells via various receptors expressed on the cell. The best studied example is DC-SIGN (usually on MDC subset 1, but other subsets under certain conditions; since not all dendritic cell subsets express DC-SIGN, its exact role in sexual HIV-1 transmission is not clear). When the dendritic cell takes up HIV and then travels to the lymph node, the virus is able to move to helper T-cells, and this infection of helper T-cells is the major cause of disease. This knowledge has vastly altered our understanding of the infectious cycle of HIV since the mid-1990s, since in the infected dendritic cells, the virus possesses a reservoir which also would have to be targeted by a therapy. This infection of dendritic cells by HIV explains one mechanism by which the virus could persist after prolonged HAART . Many other viruses, such as the SARS virus seems to use DC-SIGN to 'hitchhike' to its target cells.9 However, most work with virus binding to DC-SIGN expressing cells has been conducted using in vitro derived cells such as moDCs. The physiological role of DC-SIGN in vivo is more difficult to ascertain. Altered function of dendritic cells is also known to play a major or even key role in Allergy and Autoimmune Disease s like Lupus Erythematosus . DENDRITIC CELLS IN ANIMALS OTHER THAN HUMANS The above applies to humans. In other organisms, the function of dendritic cells can differ slightly. For example, in Brown Rat s (but not mice), a subset of dendritic cells exists that displays pronounced killer cell-like activity, apparently through its entire lifespan. However, the principal function of dendritic cells as known to date is always to act as the central command and central encyclopedia of the immune response, or similar to Server s in a computer network. They collect and store the immune system's "knowledge", enabling them to instruct and direct the adaptive arms in response to challenges. Novel subpopulations of dendritic cells have been recently identified in the mouse.
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